Canonical Allele Identifier: CA1321156544
Gene: ALS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201704252T= , CM000664.2:g.201704252T= GRCh38
NC_000002.11:g.202568975T= , CM000664.1:g.202568975T= GRCh37
NC_000002.10:g.202277220T= NCBI36
NG_008775.1:g.81921A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264276.11:c.4839-34A= MANE Select ENSP00000264276.6:n.4839-34A=
ENST00000439495.6:c.*1019-34A= ENSP00000403832.2:n.*1019-34A=
ENST00000679409.1:c.*1510A= ENSP00000506531.1:n.*1510A=
ENST00000679416.1:n.6343-34A=
ENST00000679427.1:n.2476A=
ENST00000679435.1:c.4839-34A= ENSP00000505218.1:n.4839-34A=
ENST00000679516.1:c.4839-34A= ENSP00000505187.1:n.4839-34A=
ENST00000679618.1:c.*1927-34A= ENSP00000506274.1:n.*1927-34A=
ENST00000679630.1:n.6688-34A=
ENST00000679635.1:n.3067A=
ENST00000679686.1:n.4953-34A=
ENST00000679701.1:n.7831-34A=
ENST00000679916.1:c.*1187-34A= ENSP00000506172.1:n.*1187-34A=
ENST00000680000.1:c.4839-34A= ENSP00000506173.1:n.4839-34A=
ENST00000680135.1:c.*2800-34A= ENSP00000506211.1:n.*2800-34A=
ENST00000680149.1:c.*121-34A= ENSP00000506497.1:n.*121-34A=
ENST00000680163.1:c.4839-34A= ENSP00000505092.1:n.4839-34A=
ENST00000680174.1:n.5530-34A=
ENST00000680236.1:c.*1900-34A= ENSP00000506212.1:n.*1900-34A=
ENST00000680404.1:n.354-34A=
ENST00000680441.1:n.3397-34A=
ENST00000680497.1:c.4941-34A= ENSP00000505954.1:n.4941-34A=
ENST00000680508.1:c.4836-12A= ENSP00000505749.1:n.4836-12A=
ENST00000680569.1:c.*2748A= ENSP00000505522.1:n.*2748A=
ENST00000680634.1:n.1347-34A=
ENST00000680722.1:n.2639-34A=
ENST00000680726.1:c.*121-34A= ENSP00000505505.1:n.*121-34A=
ENST00000680759.1:c.4671-34A= ENSP00000505848.1:n.4671-34A=
ENST00000680814.1:c.4838+202A= ENSP00000505710.1:n.4838+202A=
ENST00000680828.1:c.*2533-34A= ENSP00000505249.1:n.*2533-34A=
ENST00000680861.1:c.4839-34A= ENSP00000505043.1:n.4839-34A=
ENST00000680927.1:c.*1019-34A= ENSP00000505473.1:n.*1019-34A=
ENST00000680939.1:n.6746A=
ENST00000681250.1:c.*1556-34A= ENSP00000505684.1:n.*1556-34A=
ENST00000681256.1:c.*2854-34A= ENSP00000505446.1:n.*2854-34A=
ENST00000681279.1:n.5705-34A=
ENST00000681307.1:n.5952-34A=
ENST00000681461.1:n.5607-34A=
ENST00000681495.1:c.2376-34A= ENSP00000506085.1:n.2376-34A=
ENST00000681558.1:c.2517-34A= ENSP00000505568.1:n.2517-34A=
ENST00000681619.1:c.4836-34A= ENSP00000505071.1:n.4836-34A=
ENST00000681663.1:n.1745-34A=
ENST00000681692.1:n.2799-34A=
ENST00000681716.1:c.*2693-34A= ENSP00000505078.1:n.*2693-34A=
ENST00000681768.1:c.*2503-34A= ENSP00000506311.1:n.*2503-34A=
ENST00000681808.1:c.4662-34A= ENSP00000505219.1:n.4662-34A=
ENST00000264276.10:c.4839-34A= ENSP00000264276.6:n.4839-34A=
ENST00000439495.5:c.2943-34A=
NM_020919.3:c.4839-34A= NP_065970.2:n.4839-34A=
XM_005246709.2:c.4836-34A= XP_005246766.1:n.4836-34A=
XM_006712654.1:c.4839-34A= XP_006712717.1:n.4839-34A=
XM_006712655.2:c.2775-34A= XP_006712718.1:n.2775-34A=
XM_011511530.1:c.4500-34A= XP_011509832.1:n.4500-34A=
XR_922974.1:n.5117-34A=
XM_006712654.3:c.4839-34A= XP_006712717.1:n.4839-34A=
XM_006712655.3:c.2775-34A= XP_006712718.1:n.2775-34A=
XM_017004569.2:c.4836-34A= XP_016860058.1:n.4836-34A=
XM_017004572.2:c.2457-34A= XP_016860061.1:n.2457-34A=
XM_024453024.1:c.4500-34A= XP_024308792.1:n.4500-34A=
XM_024453025.1:c.2772-34A= XP_024308793.1:n.2772-34A=
XR_001738864.2:n.4954-34A=
XR_001738865.2:n.4951-34A=
XR_001738866.2:n.5117-34A=
XR_001738867.2:n.5114-34A=
XR_002959320.1:n.4010-34A=
NM_020919.4:c.4839-34A= MANE Select NP_065970.2:n.4839-34A=